FDA Inspection 967568 — Vitalant

Vitalant — FEI 3001487806

The FDA completed an inspection of Vitalant on March 16, 2016 in Farmington, NM. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 16, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Farmington, NM (United States)